Tag | Content |
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EnhancerAtlas ID | HS105-13180 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:15910800-15912330 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUND(var.2) | MA0492.1 | chr11:15912040-15912055 | AGTAATGAGGTCATA | + | 6.4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I015889 | chr11 | 15911073 | 15912320 |
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Enhancer Sequence | AGGGAATAGA GAGGGGCTGA GAATGCTGTT TAAAGAGGGA AATTGAGGTG GCCTCTAGGA 60 GGAGGTGGCA TTTGAGCCAA GATTCATTAA GTGCTGAGGG AATCTATGTA GTTATCTCGG 120 GGAAAAAGCA TTCCAGGTGA GGAATCAGCA GGTGCAAAGG CCCTGAGACA GGAGCTTCTT 180 TAGGAATGGC AAAGAAGCTG GCTGCCAGCA AAACACATGC AGGAAATCTA ACTGGAGATG 240 AGAGGGAAGA TGCAGCCAGG GCAGATCACT TAGGGTGTGG CAGCCCATGG CAACGGCTTC 300 AGCTTTTATT CTAAGCATCC CAAGTTGTGT ACAGAGAGAT AACAAGTTCA GACTTCAGTT 360 TAAAGTCCTT GTGTGGCTGC TCTTTGGGGA ACAGATTGGC AGGGTCAAGC AGAAGCTGGG 420 AGTTCAGTAA GGAGCAAATG AGCTCAGCAA ATCCTGCAGC ACCCCTATAA GATAGGTCCT 480 ATGATTATAA GGCAATGGAG GCTCAGAGAG ATTAAAGAAC TTGATCTAAG TCTCCTGCTG 540 GTATGTGGAC AGGCTGAGAG TGAACCCACA TTTGACCAAA GCCTGAGCTG CCCTAGGGCT 600 GAAAGCTCAA AGACCCAAAG ACACCATGTA AAAGGGCCCT GGTTGCTGTC TTTAAGGCAC 660 AAAGCTCTCT TATTTCAGGC TTGCTCCTAA CCAGATACCC TGAGCCTTGG TTTACTTTAG 720 AGCCACCATT TACATGGGCC TTACTGTGTC CCAGGCACAG GCTGGGACTT TGACATACAG 780 GATCTCATTT AATCCTCACT GCAGCCCAGG GAGCGGGGTA TTATTATCCC TGTGTTACCA 840 GATGAAAAAG ATCTCATTTT CTCAGTGGAG ATAGTGAAAA CATTCCAAAG CTGCTTTGGG 900 GTTTAATTCA CAGAAACCTC CGCATTTAAT CTACTAAACC AGAAAGTAAT CCTCTCTTTG 960 GCCGGCCCTG GCAGCCTGGG TCTGCCCACA GTCGTCAGAG GGAATTGGTA GCTCACACTT 1020 GCACACGTGT GCACCCACAC ACACATTCCA GGATCCAAAC CCCAGCCCAT CCTGAACCAT 1080 CCAAAAGGTG CCAGCCACCC TCACTGTGAA TGTGTCTTTA ATGCTCCCCT CCCCTTCCGC 1140 TCCAAAGCCC TTCTCCCTCC TCTGTGCACA CTCAGCCAAT GGCCTTCCTC AGGCCACCTG 1200 GCAGCCCCCA AAGCCCACTC TCTATGCTAA CTCTGGCAGC AGTAATGAGG TCATACCCAT 1260 TCCACCCCTC ACAGAACACT GCACCCTCTG GCCCAGTCCT CTCTCCTCCC TTCTCTCAGC 1320 CTCATCCAGA CCTACCCGAC CTATGTCTGT GTTTTCCAGA ACCCTGCATA ACTAACGTGA 1380 CAAGCTGTGC TGGACTCGGT TGCAAATGGC TGCCAGGAAG TTATTGATAC TAAAATCTCA 1440 GGTAATCCTT TTGGCTTTCA AAGGCACGTT CTCTGACAAT CATTTGTTCC TAGGCAGTGA 1500 AGATAATGGA GAATGATGCT GCTTGTGGCA 1530
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